Managed Access Programs for AIN457, Secukinumab
NCT05583604 · Status: AVAILABLE · Type: EXPANDED_ACCESS
Last updated 2025-12-18
Summary
The purpose of this registration is to list Managed Access Programs (MAPs) related to AIN457, secukinumab
Conditions
- Hidradenitis Suppurativa (HS)
Interventions
- DRUG
-
secukinumab
Patients receive secukinumab
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Novartis Pharmaceuticals · Novartis Pharmaceuticals
Eligibility
- Min Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
More Related Trials
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Extension Study to Assess Effects of Non-interrupted Versus Interrupted and Long Term Treatment of Two Dose Regimes of Secukinumab in Subjects With Hidradenitis Suppurativa
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Efficacy and Safety of SCT650C in Participants With Moderate to Severe Hidradenitis Suppurativa
NCT07244510 ·Status: RECRUITING ·Phase: PHASE2
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A Randomized Trial Comparing the Efficacy and Safety of Secukinumab with Tofacitinib in the Treatment of Moderate to Severe Hidradenitis Suppurativa in Chinese Patients
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Study to Collect in a Real-world populatIon Data on the Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe Hidradenitis Suppurativa (HS) in Routine Clinical Practice in the Russian Federation
NCT06517732 ·Status: ACTIVE_NOT_RECRUITING
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Efficacy and Safety Study of BDB-001 Injection in Patients With Moderate to Severe Hidradenitis Suppurativa (HS)
NCT05093855 ·Status: COMPLETED ·Phase: PHASE2
-
Short-term Treatment Satisfaction in Hidradenitis Suppurativa Patients Initiated on Cosentyx in Routine Clinical Practice in Saudi Arabia
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-
A Study Investigating Long-term Treatment With Spesolimab in People With a Skin Disease Called Hidradenitis Suppurativa Who Completed a Previous Clinical Trial
NCT04876391 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Single Doses of SBT777101 in Subjects With Hidradenitis Suppurativa
NCT06361836 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
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A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-981) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy and Who Are Naïve to Biologic Therapy
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-
Open Label Study to Assess the Effect of Secukinumab in Moderate to Severe Papulopustular Rosacea
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A Study of Zasocitinib in Adults With Hidradenitis Suppurativa
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A Study to Explore the Safety, Tolerability, Efficacy, and Pharmacokinetics of LT-002-158 Tablets in Chinese Adult Patients With Hidradenitis Suppurativa
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Study to Evaluate Tulisokibart for Hidradenitis Suppurativa (MK-7240-012)
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-
Intralesional Diode Laser Treatment of Fistulas in Hidradenitis Suppurativa
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-
Capsule Microbiota Transplant Therapy for Hidradenitis Suppurativa
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Study to Compare Two Treatments for Axillary Hidradenitis Suppurativa: Carbon Dioxide Laser Versus Surgical Deroofing
NCT02163746 ·Status: COMPLETED ·Phase: NA
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Gentian Violet Treatment for Hidradenitis Suppurativa
NCT04388163 ·Status: WITHDRAWN ·Phase: PHASE2
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Study of the Immunomodulation in the Hidradenitis Suppurativa and Evaluation of a New Therapeutic Strategy
NCT05208099 ·Status: NOT_YET_RECRUITING
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Safety, Tolerability, Pharmacokinetics, Immunogenicity and Efficacy of STP705 in Adult Patients With Hypertrophic Scars
NCT05196373 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
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Safety and Treatment of Cryoinsufflation in Treatment of Hidradenitis Suppurativa
NCT05830149 ·Status: TERMINATED ·Phase: NA
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Brivekimig for the Treatment of Moderate to Severe Hidradenitis Suppurativa
NCT07170917 ·Status: RECRUITING ·Phase: PHASE2
-
Safety and Efficacy Study of BDB-001 Injection in Patients With Moderate to Severe Hidradenitis Suppurativa (HS)
NCT05103423 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Treatment of Epidermoid Cysts
NCT05597995 ·Status: UNKNOWN ·Phase: PHASE2
-
Feasibility Study on Radiofrequency-Based Selective Electrothermolysis to Investigate Its Effects on Human Skin
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-
A Study to Evaluate RIST4721 in Hidradenitis Suppurativa (HS)
NCT05348681 ·Status: TERMINATED ·Phase: PHASE2